renal amyloidosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of amyloidosis that affects the kidney. (Human Phenotype Ontology, HP_0001917)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001917
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Genes

3 genes associated with the renal amyloidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APOA1 apolipoprotein A-I
MEFV Mediterranean fever
NLRP3 NLR family, pyrin domain containing 3